Jules Stein Eye Institute, University of California, Los Angeles, CA 94143, USA.
Int J Mol Sci. 2021 Nov 5;22(21):11975. doi: 10.3390/ijms222111975.
Limbal epithelial stem/progenitor cells (LSCs) reside in a niche that contains finely tuned balances of various signaling pathways including Wnt, Notch, BMP, Shh, YAP, and TGFβ. The activation or inhibition of these pathways is frequently dependent on the interactions of LSCs with various niche cell types and extracellular substrates. In addition to receiving molecular signals from growth factors, cytokines, and other soluble molecules, LSCs also respond to their surrounding physical structure via mechanotransduction, interaction with the ECM, and interactions with other cell types. Damage to LSCs or their niche leads to limbal stem cell deficiency (LSCD). The field of LSCD treatment would greatly benefit from an understanding of the molecular regulation of LSCs in vitro and in vivo. This review synthesizes current literature around the niche factors and signaling pathways that influence LSC function. Future development of LSCD therapies should consider all these niche factors to achieve improved long-term restoration of the LSC population.
角膜缘上皮干细胞/祖细胞(LSCs)位于一个龛位中,其中包含各种信号通路的精细平衡,包括 Wnt、Notch、BMP、Shh、YAP 和 TGFβ。这些通路的激活或抑制通常取决于 LSCs 与各种龛位细胞类型和细胞外基质的相互作用。除了从生长因子、细胞因子和其他可溶性分子接收分子信号外,LSCs 还通过机械转导、与细胞外基质的相互作用以及与其他细胞类型的相互作用来响应其周围的物理结构。LSCs 或其龛位的损伤会导致角膜缘干细胞缺陷(LSCD)。如果能深入了解 LSCs 在体外和体内的分子调控,那么 LSCD 的治疗领域将受益匪浅。这篇综述综合了目前关于影响 LSC 功能的龛位因子和信号通路的文献。未来 LSCD 治疗方法的发展应考虑所有这些龛位因素,以实现对 LSC 群体的长期改善恢复。